具有碳氟化合物/碳氢化合物混合链的油溶性含氟表面活性剂的设计、合成和结构-活性关系

IF 2.2 4区 化学 Q2 Engineering Chemical Papers Pub Date : 2024-09-09 DOI:10.1007/s11696-024-03656-3
Wen-Hai Wu, Ya-Qing Zhou, Yong Sun, Ji-Li Wang, Zhi-Qiang Xiang, Jiang Duan
{"title":"具有碳氟化合物/碳氢化合物混合链的油溶性含氟表面活性剂的设计、合成和结构-活性关系","authors":"Wen-Hai Wu,&nbsp;Ya-Qing Zhou,&nbsp;Yong Sun,&nbsp;Ji-Li Wang,&nbsp;Zhi-Qiang Xiang,&nbsp;Jiang Duan","doi":"10.1007/s11696-024-03656-3","DOIUrl":null,"url":null,"abstract":"<div><p>This study presents an exploration into the relationship between the molecular structure of oil-soluble fluorinated surfactants and their surface properties across a variety of organic solvents. A series of oil-soluble surfactants with fluorocarbon/hydrocarbon hybrid chains, <i>N</i>-methyl-<i>N</i>-alkyl-4-perfluoroalkylsulfoxybenzylamines (FmHn), were designed and synthesized, and their surface activity was evaluated in 12 organic solvents with different polarities. The surface parameters, including CMC, <span>\\({\\gamma }_{CMC}\\)</span>, <span>\\({\\Gamma }_{max}\\)</span> and <span>\\({A}_{min}\\)</span>, were measured in <i>n</i>-hexadecane, <i>m</i>-xylene, and DMSO, allowing for an in-depth analysis of the influence of molecular structure on these surface properties. Results indicate that an increase in the length of the fluorocarbon chain generally enhances surface activity, leading to a reduction in the CMC value and an increase in the effectiveness of surface tension reduction. However, the impact of the hydrocarbon chain length on surface activity is more complex and dependent on the polarity of the organic solvents. In low-polarity solvents, surface activity is improved with a longer hydrocarbon chain, whereas in high-polarity solvents, a shorter hydrocarbon chain is more beneficial. Consequently, a “polarity–directionality” strategy was proposed to tailor the molecular structure of surfactants to optimize performance in solvents with varying polarities, resulting in a significant reduction in surface tension. Specifically, F8H12 was identified as particularly effective in low-polarity n-alkanes and cycloalkanes, F6H8 was most effective in medium polarity aromatics, and F8H4 or F6H4 was ideal for larger polar solvents. These findings enrich the understanding of the structure–activity relationship in oil-soluble fluorinated surfactants and offer new perspectives for the development of high-performance surfactants with reduced environmental impact.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":513,"journal":{"name":"Chemical Papers","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Design, synthesis, and structure–activity relationships of oil-soluble fluorinated surfactants with fluorocarbon/hydrocarbon hybrid chain\",\"authors\":\"Wen-Hai Wu,&nbsp;Ya-Qing Zhou,&nbsp;Yong Sun,&nbsp;Ji-Li Wang,&nbsp;Zhi-Qiang Xiang,&nbsp;Jiang Duan\",\"doi\":\"10.1007/s11696-024-03656-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This study presents an exploration into the relationship between the molecular structure of oil-soluble fluorinated surfactants and their surface properties across a variety of organic solvents. A series of oil-soluble surfactants with fluorocarbon/hydrocarbon hybrid chains, <i>N</i>-methyl-<i>N</i>-alkyl-4-perfluoroalkylsulfoxybenzylamines (FmHn), were designed and synthesized, and their surface activity was evaluated in 12 organic solvents with different polarities. The surface parameters, including CMC, <span>\\\\({\\\\gamma }_{CMC}\\\\)</span>, <span>\\\\({\\\\Gamma }_{max}\\\\)</span> and <span>\\\\({A}_{min}\\\\)</span>, were measured in <i>n</i>-hexadecane, <i>m</i>-xylene, and DMSO, allowing for an in-depth analysis of the influence of molecular structure on these surface properties. Results indicate that an increase in the length of the fluorocarbon chain generally enhances surface activity, leading to a reduction in the CMC value and an increase in the effectiveness of surface tension reduction. However, the impact of the hydrocarbon chain length on surface activity is more complex and dependent on the polarity of the organic solvents. In low-polarity solvents, surface activity is improved with a longer hydrocarbon chain, whereas in high-polarity solvents, a shorter hydrocarbon chain is more beneficial. Consequently, a “polarity–directionality” strategy was proposed to tailor the molecular structure of surfactants to optimize performance in solvents with varying polarities, resulting in a significant reduction in surface tension. Specifically, F8H12 was identified as particularly effective in low-polarity n-alkanes and cycloalkanes, F6H8 was most effective in medium polarity aromatics, and F8H4 or F6H4 was ideal for larger polar solvents. These findings enrich the understanding of the structure–activity relationship in oil-soluble fluorinated surfactants and offer new perspectives for the development of high-performance surfactants with reduced environmental impact.</p><h3>Graphical Abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":513,\"journal\":{\"name\":\"Chemical Papers\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Papers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11696-024-03656-3\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Papers","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11696-024-03656-3","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Engineering","Score":null,"Total":0}
引用次数: 0

摘要

本研究探讨了油溶性含氟表面活性剂的分子结构与其在各种有机溶剂中的表面特性之间的关系。研究设计并合成了一系列具有氟碳/烃混合链的油溶性表面活性剂--N-甲基-N-烷基-4-全氟烷基磺氧基苄胺(FmHn),并在 12 种不同极性的有机溶剂中评估了它们的表面活性。在正十六烷、间二甲苯和二甲基亚砜中测量了包括 CMC、\({\gamma }_{CMC}\)、\({\gamma }_{max}\)和\({A}_{min}\)在内的表面参数,从而深入分析了分子结构对这些表面性质的影响。结果表明,碳氟化合物链长度的增加通常会提高表面活性,从而降低 CMC 值,提高降低表面张力的效果。不过,碳氢链长度对表面活性的影响更为复杂,取决于有机溶剂的极性。在低极性溶剂中,烃链越长,表面活性越好,而在高极性溶剂中,烃链越短,表面活性越好。因此,有人提出了一种 "极性定向 "策略,通过调整表面活性剂的分子结构来优化其在不同极性溶剂中的性能,从而显著降低表面张力。具体来说,F8H12 在低极性的正构烷烃和环烷烃中特别有效,F6H8 在中等极性的芳烃中最有效,而 F8H4 或 F6H4 则是较大极性溶剂的理想选择。这些发现丰富了人们对油溶性含氟表面活性剂结构-活性关系的认识,为开发对环境影响更小的高性能表面活性剂提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Design, synthesis, and structure–activity relationships of oil-soluble fluorinated surfactants with fluorocarbon/hydrocarbon hybrid chain

This study presents an exploration into the relationship between the molecular structure of oil-soluble fluorinated surfactants and their surface properties across a variety of organic solvents. A series of oil-soluble surfactants with fluorocarbon/hydrocarbon hybrid chains, N-methyl-N-alkyl-4-perfluoroalkylsulfoxybenzylamines (FmHn), were designed and synthesized, and their surface activity was evaluated in 12 organic solvents with different polarities. The surface parameters, including CMC, \({\gamma }_{CMC}\), \({\Gamma }_{max}\) and \({A}_{min}\), were measured in n-hexadecane, m-xylene, and DMSO, allowing for an in-depth analysis of the influence of molecular structure on these surface properties. Results indicate that an increase in the length of the fluorocarbon chain generally enhances surface activity, leading to a reduction in the CMC value and an increase in the effectiveness of surface tension reduction. However, the impact of the hydrocarbon chain length on surface activity is more complex and dependent on the polarity of the organic solvents. In low-polarity solvents, surface activity is improved with a longer hydrocarbon chain, whereas in high-polarity solvents, a shorter hydrocarbon chain is more beneficial. Consequently, a “polarity–directionality” strategy was proposed to tailor the molecular structure of surfactants to optimize performance in solvents with varying polarities, resulting in a significant reduction in surface tension. Specifically, F8H12 was identified as particularly effective in low-polarity n-alkanes and cycloalkanes, F6H8 was most effective in medium polarity aromatics, and F8H4 or F6H4 was ideal for larger polar solvents. These findings enrich the understanding of the structure–activity relationship in oil-soluble fluorinated surfactants and offer new perspectives for the development of high-performance surfactants with reduced environmental impact.

Graphical Abstract

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Chemical Papers
Chemical Papers Chemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍: Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.
期刊最新文献
Chalky limestone as sustainable water purification from eriochrome black T: kinetics, isotherm, and equilibrium O-Allyloxy chalcone derivatives: design, synthesis, anticancer activity, network pharmacology and molecular docking Natural and synthetic polymers as effective corrosion inhibitors: a concise review Development of molecularly imprinted polymer-based dispersive micro-solid-phase extraction for the selective extraction of histamine from canned tuna fish samples prior to its determination by GC–FID Virtual screening, docking, molecular dynamics study of efflux pump inhibitors against Helicobacter pylori
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1